Altered Bone Status in Rett Syndrome
Altered Bone Status in Rett Syndrome
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Publisher
Basel: MDPI AG
Journal title
Language
English
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Publication information
Publisher
Basel: MDPI AG
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Scope and Contents
Contents
Rett syndrome (RTT) is a monogenic neurodevelopmental disorder primarily caused by mutations in X-linked MECP2 gene, encoding for methyl-CpG binding protein 2 (MeCP2), a multifaceted modulator of gene expression and chromatin organization. Based on the type of mutation, RTT patients exhibit a broad spectrum of clinical phenotypes with various degre...
Alternative Titles
Full title
Altered Bone Status in Rett Syndrome
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TN_cdi_doaj_primary_oai_doaj_org_article_3dc2f2587c8a489e904660c7fb833bb3
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3dc2f2587c8a489e904660c7fb833bb3
Other Identifiers
ISSN
2075-1729
E-ISSN
2075-1729
DOI
10.3390/life11060521
